Canonical Allele Identifier: PA658659134
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449125
ClinVar RCV Id: RCV000520823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Ile587Thr
CA346365446
NM_005633.4:c.1760T>C